Difference between revisions of "Part:BBa K2611010"
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We added a spacer sequence and a NGG site closely before the promoter([https://parts.igem.org/Part:BBa_J23101 BBa_J23101] | We added a spacer sequence and a NGG site closely before the promoter([https://parts.igem.org/Part:BBa_J23101 BBa_J23101] | ||
− | ). This spacer sequence can be recognized by the sgRNA we designed to direct dCas9. Once dCas9 binds with the spacer sequence, the expression of GFP will be repressed.We have submitted the sgRNA part (BBa_K2611000) and spacer-GFP part(BBa_K2611001). In this composite part, we linked them together.We observed positive colonies transformed with | + | ). This spacer sequence can be recognized by the sgRNA we designed to direct dCas9. Once dCas9 binds with the spacer sequence, the expression of GFP will be repressed.We have submitted the sgRNA part ([https://parts.igem.org/Part:BBa_K2611000 BBa_K2611000]) and spacer-GFP part(BBa_K2611001). In this composite part, we linked them together.We observed positive colonies transformed with this part under a stereo fluorescence microscope.Green fluorescence was observed.(Fig.1) |
[[File:Long description.png]] | [[File:Long description.png]] |
Revision as of 12:26, 17 October 2018
sgRNA(spacer J23101-GFP)-spacer J23101-GFP
We added a spacer sequence and a NGG site closely before the promoter(BBa_J23101 ). This spacer sequence can be recognized by the sgRNA we designed to direct dCas9. Once dCas9 binds with the spacer sequence, the expression of GFP will be repressed.We have submitted the sgRNA part (BBa_K2611000) and spacer-GFP part(BBa_K2611001). In this composite part, we linked them together.We observed positive colonies transformed with this part under a stereo fluorescence microscope.Green fluorescence was observed.(Fig.1)
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 226
Illegal NheI site found at 249 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 924